Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000974 | Prp19 complex | 2 | 1 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: E9AR48
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 1 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 1 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008380 | RNA splicing | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 260 | 264 | PF00656 | 0.709 |
CLV_C14_Caspase3-7 | 313 | 317 | PF00656 | 0.589 |
CLV_C14_Caspase3-7 | 397 | 401 | PF00656 | 0.491 |
CLV_C14_Caspase3-7 | 450 | 454 | PF00656 | 0.716 |
CLV_C14_Caspase3-7 | 537 | 541 | PF00656 | 0.622 |
CLV_C14_Caspase3-7 | 547 | 551 | PF00656 | 0.616 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 502 | 504 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 570 | 572 | PF00675 | 0.693 |
CLV_NRD_NRD_1 | 777 | 779 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.277 |
CLV_PCSK_FUR_1 | 148 | 152 | PF00082 | 0.455 |
CLV_PCSK_FUR_1 | 802 | 806 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 483 | 485 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 570 | 572 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 777 | 779 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 804 | 806 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.277 |
CLV_PCSK_PC1ET2_1 | 435 | 437 | PF00082 | 0.636 |
CLV_PCSK_PC1ET2_1 | 483 | 485 | PF00082 | 0.577 |
CLV_PCSK_PC1ET2_1 | 804 | 806 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 631 | 635 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 707 | 711 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 771 | 775 | PF00082 | 0.568 |
DEG_APCC_DBOX_1 | 333 | 341 | PF00400 | 0.606 |
DEG_APCC_DBOX_1 | 437 | 445 | PF00400 | 0.636 |
DEG_APCC_DBOX_1 | 776 | 784 | PF00400 | 0.519 |
DEG_SPOP_SBC_1 | 323 | 327 | PF00917 | 0.533 |
DEG_SPOP_SBC_1 | 473 | 477 | PF00917 | 0.696 |
DEG_SPOP_SBC_1 | 542 | 546 | PF00917 | 0.771 |
DEG_SPOP_SBC_1 | 584 | 588 | PF00917 | 0.569 |
DOC_CKS1_1 | 594 | 599 | PF01111 | 0.647 |
DOC_MAPK_DCC_7 | 436 | 446 | PF00069 | 0.717 |
DOC_PP1_RVXF_1 | 1 | 7 | PF00149 | 0.540 |
DOC_PP2B_LxvP_1 | 429 | 432 | PF13499 | 0.648 |
DOC_PP2B_LxvP_1 | 497 | 500 | PF13499 | 0.651 |
DOC_PP2B_LxvP_1 | 738 | 741 | PF13499 | 0.658 |
DOC_PP4_MxPP_1 | 425 | 428 | PF00568 | 0.651 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 536 | 540 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 602 | 606 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 648 | 652 | PF00917 | 0.672 |
DOC_USP7_MATH_2 | 135 | 141 | PF00917 | 0.417 |
DOC_USP7_UBL2_3 | 192 | 196 | PF12436 | 0.485 |
DOC_USP7_UBL2_3 | 392 | 396 | PF12436 | 0.612 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 586 | 591 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 593 | 598 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 614 | 619 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 700 | 705 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 720 | 725 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.477 |
LIG_14-3-3_CanoR_1 | 33 | 38 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 346 | 352 | PF00244 | 0.709 |
LIG_14-3-3_CanoR_1 | 368 | 377 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 647 | 653 | PF00244 | 0.632 |
LIG_APCC_ABBA_1 | 277 | 282 | PF00400 | 0.539 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.552 |
LIG_BIR_III_4 | 129 | 133 | PF00653 | 0.599 |
LIG_BIR_III_4 | 316 | 320 | PF00653 | 0.628 |
LIG_BRCT_BRCA1_1 | 361 | 365 | PF00533 | 0.643 |
LIG_EVH1_1 | 429 | 433 | PF00568 | 0.649 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.453 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.501 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.642 |
LIG_FHA_1 | 494 | 500 | PF00498 | 0.594 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.599 |
LIG_FHA_1 | 763 | 769 | PF00498 | 0.499 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.477 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.472 |
LIG_FHA_2 | 445 | 451 | PF00498 | 0.748 |
LIG_FHA_2 | 476 | 482 | PF00498 | 0.537 |
LIG_FHA_2 | 554 | 560 | PF00498 | 0.606 |
LIG_FHA_2 | 586 | 592 | PF00498 | 0.703 |
LIG_FHA_2 | 594 | 600 | PF00498 | 0.692 |
LIG_FHA_2 | 615 | 621 | PF00498 | 0.667 |
LIG_FHA_2 | 794 | 800 | PF00498 | 0.480 |
LIG_LIR_Apic_2 | 51 | 56 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 106 | 115 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 271 | 280 | PF02991 | 0.593 |
LIG_LIR_Gen_1 | 30 | 38 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 400 | 410 | PF02991 | 0.554 |
LIG_LIR_Gen_1 | 492 | 502 | PF02991 | 0.576 |
LIG_LIR_Gen_1 | 692 | 701 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 30 | 34 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 400 | 406 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 48 | 53 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 492 | 497 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 692 | 696 | PF02991 | 0.510 |
LIG_Pex14_2 | 79 | 83 | PF04695 | 0.474 |
LIG_SH2_PTP2 | 98 | 101 | PF00017 | 0.410 |
LIG_SH2_SRC | 53 | 56 | PF00017 | 0.541 |
LIG_SH2_STAT3 | 119 | 122 | PF00017 | 0.433 |
LIG_SH2_STAT3 | 280 | 283 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 713 | 716 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 746 | 749 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.410 |
LIG_SH3_2 | 430 | 435 | PF14604 | 0.651 |
LIG_SH3_2 | 466 | 471 | PF14604 | 0.667 |
LIG_SH3_3 | 424 | 430 | PF00018 | 0.642 |
LIG_SH3_3 | 463 | 469 | PF00018 | 0.767 |
LIG_SUMO_SIM_par_1 | 442 | 447 | PF11976 | 0.719 |
LIG_TRAF2_1 | 157 | 160 | PF00917 | 0.461 |
LIG_TRAF2_1 | 234 | 237 | PF00917 | 0.496 |
LIG_TRAF2_1 | 391 | 394 | PF00917 | 0.614 |
LIG_TRAF2_1 | 447 | 450 | PF00917 | 0.716 |
LIG_TRAF2_1 | 65 | 68 | PF00917 | 0.477 |
LIG_WRC_WIRS_1 | 141 | 146 | PF05994 | 0.521 |
LIG_WW_2 | 427 | 430 | PF00397 | 0.692 |
MOD_CDK_SPxxK_3 | 700 | 707 | PF00069 | 0.562 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.527 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.666 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.773 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.315 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.598 |
MOD_CK1_1 | 475 | 481 | PF00069 | 0.655 |
MOD_CK1_1 | 762 | 768 | PF00069 | 0.474 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.478 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.461 |
MOD_CK2_1 | 355 | 361 | PF00069 | 0.646 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.720 |
MOD_CK2_1 | 475 | 481 | PF00069 | 0.668 |
MOD_CK2_1 | 553 | 559 | PF00069 | 0.612 |
MOD_CK2_1 | 585 | 591 | PF00069 | 0.720 |
MOD_CK2_1 | 593 | 599 | PF00069 | 0.681 |
MOD_CK2_1 | 602 | 608 | PF00069 | 0.597 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.315 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.315 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.514 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.499 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.635 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.720 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.576 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.719 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.782 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.517 |
MOD_GlcNHglycan | 546 | 549 | PF01048 | 0.674 |
MOD_GlcNHglycan | 612 | 615 | PF01048 | 0.729 |
MOD_GlcNHglycan | 697 | 700 | PF01048 | 0.446 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.479 |
MOD_GlcNHglycan | 728 | 731 | PF01048 | 0.686 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.555 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.483 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.661 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.751 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.673 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.724 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.456 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.645 |
MOD_GSK3_1 | 579 | 586 | PF00069 | 0.488 |
MOD_GSK3_1 | 610 | 617 | PF00069 | 0.721 |
MOD_GSK3_1 | 627 | 634 | PF00069 | 0.574 |
MOD_GSK3_1 | 789 | 796 | PF00069 | 0.542 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.345 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.448 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.507 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.675 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.593 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.694 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.621 |
MOD_NEK2_2 | 221 | 226 | PF00069 | 0.504 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.320 |
MOD_PIKK_1 | 631 | 637 | PF00454 | 0.692 |
MOD_PIKK_1 | 669 | 675 | PF00454 | 0.599 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.478 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.506 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.706 |
MOD_PKA_2 | 578 | 584 | PF00069 | 0.613 |
MOD_PKA_2 | 762 | 768 | PF00069 | 0.537 |
MOD_PKB_1 | 757 | 765 | PF00069 | 0.520 |
MOD_Plk_1 | 452 | 458 | PF00069 | 0.723 |
MOD_Plk_1 | 793 | 799 | PF00069 | 0.503 |
MOD_Plk_2-3 | 137 | 143 | PF00069 | 0.579 |
MOD_Plk_2-3 | 62 | 68 | PF00069 | 0.315 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.527 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.315 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.646 |
MOD_Plk_4 | 602 | 608 | PF00069 | 0.548 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.696 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.640 |
MOD_ProDKin_1 | 586 | 592 | PF00069 | 0.698 |
MOD_ProDKin_1 | 593 | 599 | PF00069 | 0.651 |
MOD_ProDKin_1 | 614 | 620 | PF00069 | 0.524 |
MOD_ProDKin_1 | 700 | 706 | PF00069 | 0.613 |
MOD_ProDKin_1 | 720 | 726 | PF00069 | 0.688 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.315 |
MOD_SUMO_for_1 | 112 | 115 | PF00179 | 0.384 |
MOD_SUMO_for_1 | 209 | 212 | PF00179 | 0.459 |
MOD_SUMO_for_1 | 391 | 394 | PF00179 | 0.614 |
MOD_SUMO_rev_2 | 278 | 286 | PF00179 | 0.557 |
MOD_SUMO_rev_2 | 390 | 398 | PF00179 | 0.529 |
MOD_SUMO_rev_2 | 475 | 485 | PF00179 | 0.534 |
MOD_SUMO_rev_2 | 65 | 73 | PF00179 | 0.315 |
TRG_DiLeu_BaEn_1 | 301 | 306 | PF01217 | 0.439 |
TRG_DiLeu_BaEn_1 | 68 | 73 | PF01217 | 0.315 |
TRG_DiLeu_BaLyEn_6 | 81 | 86 | PF01217 | 0.315 |
TRG_DiLeu_LyEn_5 | 301 | 306 | PF01217 | 0.439 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.370 |
TRG_ER_diArg_1 | 148 | 151 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 570 | 572 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 757 | 760 | PF00400 | 0.693 |
TRG_ER_diArg_1 | 776 | 778 | PF00400 | 0.396 |
TRG_NES_CRM1_1 | 666 | 681 | PF08389 | 0.411 |
TRG_NLS_MonoExtC_3 | 228 | 233 | PF00514 | 0.503 |
TRG_NLS_MonoExtN_4 | 226 | 233 | PF00514 | 0.504 |
TRG_Pf-PMV_PEXEL_1 | 233 | 237 | PF00026 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 293 | 298 | PF00026 | 0.498 |
TRG_Pf-PMV_PEXEL_1 | 304 | 308 | PF00026 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 778 | 782 | PF00026 | 0.539 |
TRG_Pf-PMV_PEXEL_1 | 795 | 799 | PF00026 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 84 | 88 | PF00026 | 0.315 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKC2 | Leptomonas seymouri | 53% | 100% |
A0A3S7WUG8 | Leishmania donovani | 92% | 100% |
A4H921 | Leishmania braziliensis | 83% | 100% |
A4HXF3 | Leishmania infantum | 92% | 100% |
Q4QEB5 | Leishmania major | 90% | 100% |